A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262923



Internal ID20829963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72958442..72958631hg38UCSC Ensembl
chr3:73007593..73007782hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553615
Supporting Variants
Samples
Known GenesGXYLT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262923
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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